Canonical Allele Identifier: CA464450867
Gene: RMRP HGNC NCBI

Linked Data

ClinVar Variation Id: 1938581
ClinVar RCV Id: RCV002662709
gnomAD v4: 9-35657946-T-C
MyVariant Identifiers: chr9:g.35657943T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657946T>C , CM000671.2:g.35657946T>C GRCh38
NC_000009.11:g.35657943T>C , CM000671.1:g.35657943T>C GRCh37
NC_000009.10:g.35647943T>C NCBI36
NG_017041.1:g.5073A>G , LRG_163:g.5073A>G
NG_033120.1:g.4657T>C

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.73A>G , LRG_163t1:n.73A>G
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